Meredith Curtis

710 total citations
10 papers, 194 citations indexed

About

Meredith Curtis is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pharmacology. According to data from OpenAlex, Meredith Curtis has authored 10 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Pharmacology. Recurrent topics in Meredith Curtis's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (2 papers). Meredith Curtis is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (2 papers). Meredith Curtis collaborates with scholars based in Canada, United States and United Kingdom. Meredith Curtis's co-authors include Laura K. Bachrach, Jennifer L. Kelsey, Kathryn Melsop, Jeri W. Nieves, Mary Fran Sowers, Gail A. Greendale, Kristin L. Sainani, Jennifer L. Carlson, Bonnie Halpern‐Felsher and John B. A. Okello and has published in prestigious journals such as Blood, PLoS Genetics and Journal of Adolescent Health.

In The Last Decade

Meredith Curtis

9 papers receiving 188 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Meredith Curtis Canada 5 98 40 38 31 28 10 194
Oliver Heine Germany 12 111 1.1× 17 0.4× 82 2.2× 32 1.0× 5 0.2× 25 329
Utkarsh Singh Australia 9 104 1.1× 34 0.8× 20 0.5× 5 0.2× 11 0.4× 24 301
Duncan A. Raymond Canada 3 149 1.5× 21 0.5× 45 1.2× 21 0.7× 141 5.0× 4 278
Montserrat Romera Baurés Spain 8 107 1.1× 7 0.2× 52 1.4× 13 0.4× 26 0.9× 29 318
Daniel B Hall United States 6 172 1.8× 10 0.3× 114 3.0× 24 0.8× 122 4.4× 8 337
Kirsten Allen United States 7 134 1.4× 20 0.5× 46 1.2× 22 0.7× 12 0.4× 12 393
Matthias Walle United States 7 67 0.7× 32 0.8× 25 0.7× 15 0.5× 6 0.2× 15 199
Linda Denise Fernandes Moreira Brazil 6 133 1.4× 14 0.3× 87 2.3× 8 0.3× 40 1.4× 8 248
Tania Inés Nava‐Bringas Mexico 10 51 0.5× 14 0.3× 14 0.4× 8 0.3× 36 1.3× 25 238
Aravinda Ganapathy United States 7 16 0.2× 23 0.6× 209 5.5× 17 0.5× 9 0.3× 25 329

Countries citing papers authored by Meredith Curtis

Since Specialization
Citations

This map shows the geographic impact of Meredith Curtis's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Meredith Curtis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Meredith Curtis more than expected).

Fields of papers citing papers by Meredith Curtis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Meredith Curtis. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Meredith Curtis. The network helps show where Meredith Curtis may publish in the future.

Co-authorship network of co-authors of Meredith Curtis

This figure shows the co-authorship network connecting the top 25 collaborators of Meredith Curtis. A scholar is included among the top collaborators of Meredith Curtis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Meredith Curtis. Meredith Curtis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Curtis, Meredith, Thomas Nalpathamkalam, Bhooma Thiruvahindrapuram, et al.. (2025). Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants. PLoS Genetics. 21(1). e1011540–e1011540.
2.
Curtis, Meredith, et al.. (2024). A comparative medical genomics approach may facilitate the interpretation of rare missense variation. Journal of Medical Genetics. 61(8). 817–821. 3 indexed citations
3.
Ding, Qiliang, Roozbeh Manshaei, Brett Trost, et al.. (2022). SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing. Human Genetics. 142(2). 201–216. 3 indexed citations
4.
Khan, Tayyaba, Meredith Curtis, Eyal Cohen, et al.. (2022). Pharmacogenetic profiling via genome sequencing in children with medical complexity. Pediatric Research. 93(4). 905–910. 6 indexed citations
5.
Cohn, Iris, Roozbeh Manshaei, Eriskay Liston, et al.. (2021). Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting. JAMA Network Open. 4(5). e2110446–e2110446. 24 indexed citations
6.
Luca, Stephanie, Gregory Costain, Maria Marano, et al.. (2021). Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?. Journal of Genetic Counseling. 31(2). 523–533. 9 indexed citations
7.
Curtis, Meredith, Danielle Baribeau, Susan Walker, et al.. (2020). A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome. American Journal of Medical Genetics Part A. 182(9). 2145–2151. 3 indexed citations
8.
Chari, Ajai, Hearn Jay Cho, Samir Parekh, et al.. (2016). A Phase II Study of Pomalidomide, Daily Low Dose Oral Cyclophosphamide, and Dexamethasone in Relapsed/Refractory Multiple Myeloma. Blood. 128(22). 4520–4520. 4 indexed citations
9.
Nieves, Jeri W., Kathryn Melsop, Meredith Curtis, et al.. (2010). Nutritional Factors That Influence Change in Bone Density and Stress Fracture Risk Among Young Female Cross‐Country Runners. PM&R. 2(8). 740–750. 129 indexed citations
10.
Carlson, Jennifer L., Meredith Curtis, & Bonnie Halpern‐Felsher. (2007). Clinician Practices for the Management of Amenorrhea in the Adolescent and Young Adult Athlete. Journal of Adolescent Health. 40(4). 362–365. 13 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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